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  • Thionyl Chloride. INTERIM: 05/2008. 2. ACUTE EXPOSURE GUIDELINE LEVELS (AEGLs) FOR. THIONYL CHLORIDE. 7719-09-7 Thionyl Chloride. INTERIM: 05/2008. 3. 1. 2. 3. 4. PREFACE. 5. 6. Under the authority of the Federal Advisory Committee. — “Thionyl Chloride Interim AEGL Document”, epa.gov
  • PowerStream offers the following lithium thionyl batteries to original equipment manufacturers. Lithium thionyl Chloride have the highest energy density of any lithium battery. — “Single piece and bulk quantity Lithium thionyl (LiSOCl2”,
  • Suppliers List, E-mail/RFQ Form, Molecular Structure, Weight, Formula, IUPAC, Synonyms for Thionyl Chloride CAS 7719-09-7. — “Thionyl Chloride CAS 7719-09-7”,
  • The thionyl group is SO, a sulfur atom plus an oxygen atom. Thionyl chloride, SOCl2, is a common reagent used in organic synthesis to convert carboxylic acids to acyl chlorides. In organic chemistry, the thionyl group is known as a sulfoxide group, and has the general structure RS(=O)R'. — “Thionyl - Wikipedia, the free encyclopedia”,
  • China Thionyl Chloride Manufacturers Verified with 3 or more face-to-face visits by Global Sources Choose Verified China Thionyl Chloride Manufacturers & Suppliers. — “Thionyl Chloride China Manufacturers”,
  • Lithium-thionyl chloride cells have a metallic lithium anode (the lightest of all the metals) and a liquid cathode comprising a porous carbon current collector filled with thionyl chloride (SOCl2) Lithium-thionyl chloride cells have a high energy density, partly. — “Lithium-thionyl chloride (Li-SOCl2)”,
  • The thionyl group is SO, a sulfur atom plus an oxygen atom. Thionyl chloride, SOCl2, is a common reagent used in organic synthesis to convert carboxylic acids to acyl chlorides. In organic chemistry, the thionyl group is known as a sulfoxide group, and has the general structure RS(=O)R'. — “Thionyl: Information from ”,
  • Facts and figures about Thionyl chloride, taken from Freebase, the world's database. — “Thionyl chloride facts - Freebase”,
  • Occupational Safety and Health Guideline for Thionyl Chloride This guideline summarizes pertinent information about Thionyl Chloride for workers and employers as well as for physicians, industrial hygienists,. — “Occupational Safety and Health Guideline for Thionyl Chloride”, osha.gov
  • Ingredient CAS No Percent Hazardous -Thionyl Chloride 7719-09-7 90 - 100% Yes Cancer Lists\-NTP Carcinogen--- Ingredient Known Anticipated IARC Category -Thionyl Chloride (7719-09-7) No No None. — “THIONYL CHLORIDE”,
  • thionyl manufacturers directory - over 2,000,000 registered importers and exporters. thionyl manufacturers, thionyl suppliers, thionyl wholesalers, exporters, sellers, traders and thionyl Distributors from China and around the world at Tradevv. — “thionyl - offers from thionyl china manufacturers, suppliers”,
  • Thionyl chloride (7719-09-7)'s ,Uses,Safety,Toxicity,Consensus,History,Production,***yticalMethods,Standards Organism. — “Thionyl chloride (7719-09-7) ,Thionyl chloride (7719-09-7”,
  • Thionyl Manufacturers & Thionyl Suppliers Directory - Find a Thionyl Manufacturer and Supplier. Choose quality Thionyl Manufacturers, Suppliers, Exporters at . — “Thionyl-Thionyl Manufacturers, Suppliers and Exporters on”,
  • Thionyl definition, sulfinyl. See more. (modifier) Also: sulphinyl of, consisting of, or containing the divalent group SO: a thionyl group or radical; thionyl chloride. — “Thionyl | Define Thionyl at ”,
  • Inhalation of thionyl chloride may result in pulmonary edema. 173.185. All lithium/thionyl chloride cells with a lithium or lithium alloy content of greater than 0.5 are restricted and. — “Lithium Thionyl Chloride”,
  • Battery Chemistries: Lithium Thionyl Chloride. Use our Li-ion battery calculator and builder to find out what configuration your application requires and get a quote. Lithium thionyl chloride batteries are best where long storage life, high energy density. — “Rose : Battery Chemistries -- Lithium Thionyl”,
  • Thionyl Chloride is a CORROSIVE CHEMICAL and. contact can severely irritate and burn the Breathing Thionyl Chloride can irritate the lungs causing. — “THIONYL CHLORIDE”, nj.gov
  • Welcome to where your battery and charger needs for computer backup systems, digital cameras, camcorders, game systems, motorcycles, ATV's, cell phones, PDA's, GPS navigation devices, laptops, alarm remote controls, flashlights,. — “ - Lithium Thionyl Chloride Batteries for”,
  • Other names: Sulfinyl chloride; Sulfur chloride oxide (Cl2SO); Sulfurous dichloride; Sulfurous oxychloride; Thionyl dichloride; SOCl2; Sulfur chloride oxide; UN 1836; Sulfinyl dichloride; Sulfur chloride oxide (scl2o); Sulfur oxychloride; Sulfur oxychloride (socl2); Thionyl chloride (socl2). — “Thionyl chloride”, webbook.nist.gov
  • Definition of thionyl from Webster's New World College Dictionary. Meaning of thionyl. Pronunciation of thionyl. Definition of the word thionyl. Origin of the word thionyl. — “thionyl - Definition of thionyl at ”,
  • Translations of thionyl. thionyl synonyms, thionyl antonyms. Information about thionyl in the free online English dictionary and encyclopedia. (Chemistry) (modifier) of, consisting of, or containing the divalent group SO a thionyl group or radical thionyl chloride Also sulphinyl. — “thionyl - definition of thionyl by the Free Online Dictionary”,
  • thionyl chloride. thionyl fluoride. thionyl iodide [edit] Synonyms thionyl" Categories: English nouns | Chemistry. Personal tools. Log in / create account. — “thionyl - Wiktionary”,

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  • ER34100 examine the original picture
  • ER17 33 ���a�u examine the original picture
  • Schedule 3 Thionyl chloride E depois ainda tem gente que diz eles os produtores não sabem o que estão fazendo Isso é uma das coisas que provam a atenção que é dada a estes detalhes em LOST Nunca existiu uma
  • The photograph on the right shows a Bat which may be attached to objects or carried by personnel a more detailed internal view can be found here Bats measure 7 5cm x 3 5cm x 1 5 cm and are powered by a single 3 6V Lithium Thionyl Chloride cell which has a lifetime of around fif*** months Each Bat has a unique 48 bit code
  • 12 18 3b Prepare thionyl chloride SOCl2 This experiment may not be allowed in some school systems See diagram 12 18 3b 1 Use 10 cc of phosphorus pentachloride in a dry distilling flask attached to a sloping condenser Fit the flask with a stopper and delivery tube that reaches deep into
  • Unlike Kyride no phthalic anhydride crystals condensed from the liquid on cooling and ***ysis showed this to be almost pure phthalyl chloride Attempted thionyl chloride synthesis from benzotrichloride and SO2 no reaction
  • ER17 50 examine the original picture
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  • Forte ER34615 ER34615M ER34615H LITHIUM THIONYL CHLORIDE BATTERY size D ER34615 ER34615M ER34615H equivalent to Tadiran TL2300 TL4930 TL5930 Saft LS 33600 LS 33600C LSH20 Sonnenschein SL 780 Tekcell SB D01 Xeno XL
  • acid by ortholithiation of benzanilide SOCl2=Thionyl chloride R NH2=Substituted aryl mine BuLi THF=n butyllithium tetrahydrofuran CuBr2=Cupper bromide CH2=CHCH 2 Br = Allyl bromide
  • 16 16 XXVIIIa as bisulphate treated with thionyl chloride and the with alcohols R OH R=Me Et Me 2 N CH 2CH 2 yields esters
  • THIONYL FLUORIDE
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  • The products after reduction to the alcohols were treated with thionyl chloride to give the chlorocompounds XLV and XLVI the latter were used in the general synthesis as before
  • life as well So don t blame Tadiran if your batteries don t last you have to design the system to protect the batteries and eliminate all leakage paths and temperature extremes Good luck This NiCd battery pack leaked at both ends Tadiran s batteries are welded and have a glass frit seal so they should not exhibit this problem And let s cheer for former tech editor and
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  • Â The second available power souce is from Lithium Thionyl Chloride non rechargeable batteries Each battery is an array of 16 D cells from SAFT with a total weight of 1 6 Kg It is
  • ***Ia the same derivative obtained 12 by the action of thionyl chloride alone on the acid XXVIIIa Similar ring closures have been reported recently 43 in another connexion Attempts 43 to prepare esters of XXVIIIb via the acid chloride led only to the pyrrolidone ***Ib

Videos
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  • Organic chemistry: Carboxylic acids (7) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Tests on lithium battery fire Lithium batteries pose a unique hazard during transport because they contain stored energy, which if released through a short circuit is capable of causing a fire.
  • Saft LS-14250 1 2 AA 3.6V Lithium Primary Battery for Mac computers click here toget 8% off discount Saft LS-14250 1/2 AA 3.6V Lithium Primary Battery for Mac computers Features and Benefits: 1/2AA size Lithium Thionyl Chloride Cylindrical Cell. High energy, high reliability 3.6 volt power source. Excellent memory backup power source. Low self discharge rate gives this cell a 10 year shelf life
  • lithium battery
  • Properties Of Ethanol Check us out at Ethanol is classified as a primary alcohol, meaning that the carbon to which its hydroxyl group is attached has at least two hydrogen atoms attached to it as well. Many of the reactions of ethanol occur at its hydroxyl group. In the presence of acid catalysts, ethanol reacts with carboxylic acids to produce ethyl esters and water: RCOOH + HOCH2CH3 → RCOOCH2CH3 + H2O This reaction, which is conducted on large scale industrially, requires the removal of the water from the reaction mixture as it is formed. Esters react in the presence of an acid or base to give back the alcohol and carboxylic acid. This reaction is known as saponification because it is used in the preparation of soap. Ethanol can also form esters with inorganic acids. Diethyl sulfate and triethyl phosphate are prepared by treating ethanol with sulfur trioxide and phosphorus pentoxide respectively. Diethyl sulfate is a useful ethylating agent in organic synthesis. Ethyl nitrite, prepared from the reaction of ethanol with sodium nitrite and sulfuric acid, was formerly a widely used diuretic. Strong acid desiccants cause the dehydration of ethanol dehydration to form diethyl ether, although under certain conditions ethylene is the product. Millions of kilograms of diethyl ether are produced annually using sulfuric acid catalyst: 2 CH3CH2OH → CH3CH2OCH2CH3 + H2O (on 120'C) Complete combustion of ethanol forms carbon dioxide and water: C2H5OH + 3 O2 → 2 CO2 + 3 H2O(l);(ΔHc ...
  • Organic chemistry: Carboxylic acids (3) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Amidification (Sorry for the res, it was recorded on my iphone). This is a ladder down reaction from an acyl chloride to an amide. The acyl chloride was prepared with my unknown carboxylic acid and thionyl chloride (SOCl2). Gotta love exothermic reactions!
  • 17 Reaction of alcohols with thionyl chloride Dehydration of alcohols Reaction of alcohols with p toluenesulfonyl chlorise 17
  • Organic chemistry: Carboxylic acids (5) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Organic chemistry: Carboxylic acids (14) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Organic chemistry: Carboxylic acids (2) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Organic chemistry: Carboxylic acids (10) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Organic chemistry: Carboxylic acids (12) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Make Sulfuric acid (metabisulfite/oxidizer method) We make concentrated sulfuric acid from sodium metabisulfite, hydrochloric acid and an oxidant such as hydrogen peroxide or nitric acid. Warning: The procedures in this video produce large quantities of toxic gases and deal with highly corrosive acids. All work must be performed in a fume hood with proper safety equipment. And all apparatus must be glass to withstand the acids. Sodium metabisulfite upon reaction with acid will generate sulfur dioxide. This provides a convenient source of sulfur dioxide that is easier to handle than burning sulfur, but it is acceptable if you want to go that route. You'll just need to build a sophisticated gas capture and scrubbing system so the sulfur vapors and soot don't clog your tubes, poison your air and possibly burn down your workspace. Sulfur dioxide is converted into sulfuric acid by reacting it with an oxidizer in water. In this case either hydrogen peroxide or nitric acid. Industrially, sulfur dioxide is reacted with oxygen over a catalyst to make sulfur trioxide. This is cheaper but extremely difficult to do safely for the home chemist so the metabisulfite/oxidizer method is used instead. You may use potassium metabisulfite instead of sodium metabisulfite. Both are used by home brewers to sterilize winemaking and beermaking mixtures. It's also used for homemade dyeing processes. Therefore it is very easy to obtain the metabisulfites without the need for expensive shipping fees or licenses. The oxidizers must be present for ...
  • Interconversion of Carboxylic Acid Derivatives After reviewing the relative reactivity of carboxylic acid derivatives, the reagent thionyl chloride is introduced to demonstrate how a carboxylic acid can be transformed to the more reactive acid chloride.
  • Litihium Ion Battery Cell Manufacturing in the US James Greenberger NATBAT An interview taped at the Grid-Connected Mobility Conference in San Francisco, CA 2009 with James Greenberger, National Alliance for Advanced Transportation Batteries or NATBAT Making Lithium Ion Cells in the US James Greenberger, National Alliance for Advanced Transportation Batteries or NATBAT, outlines the importance of making lithium ion battery cells in the United States in order to stay competitive. Bringing Battery Manufacturing to the US Lithium Ion battery cells for next generation vehicles are made almost entirely in Asia and Europe, but NATBAT is working to change that. The National Alliance for Advanced Transportation Batteries is working to ensure the US's success in the industry of lithium ion battery technology and development. Will the US take over the industry of lithium ion battery manufacturing? Or will China, Japan, and possibly South Korea take the lead in the manufacturing of the popular battery technology? Lithium Ion batteries are a technology of the future but they are also a technology of the present. Listen to James Greenberger's interview on the National Alliance for Advanced Transportation Batteries (NATBAT) regarding the manufacturing of lithium ion battery cells in the US
  • Organic chemistry: Carboxylic acids (6) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Organic chemistry: Carboxylic acids (9) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Magnesium carbon salt water battery cell A simple demonstration of a magnesium, carbon and saturated salt water solution, wet, galvanic reserve battery Cell. CAUTION: Making large surface area cells of this type of battery will produce a larger quantity of flammable and explosive hydrogen gas and a likely lesser amount of poisonous chlorine gas. Any anticipated large surface area battery cell should be stored outdoors or outside of living quarters for safety. Correction: The Anode (magnesium) (-), and the Cathode (carbon graphite) is (+). While the initial voltage and current can be relatively high, the oxidation of the magnesium, scale buildup and salt accumulation all tend to lower the cell output within a very short period of time.
  • Acid Chloride Formation Acetic Acid to Acetyl Chloride mechanism. Can be generalized to forming any acid halide from a carboxylic acid
  • Organic chemistry: Carboxylic acids (1) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the student's permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • a quick way to draw cyclic carbohydrates, the SOCl2 mech and a synthesis problem nerz at bryn mawr describes a quicker way to transform linear carbohydrates into haworth projections, the mechanism for the reaction of carboxylic acids with thionyl chloride and does an all encompassing synthesis problem involving the wittig and grigard reactions
  • Organic chemistry: Carboxylic acids (8) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Organic chemistry: Carboxylic acids (11) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Ryuichi Sakamoto-Energy Flow One of the most popular piece by Ryuichi Sakamoto. Hope he is playing a Yamaha piano ^^.
  • Organic chemistry: Carboxylic acids (13) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Organic chemistry: Carboxylic acids (4) Organic chemistry: Acidity of carboxylic acids; ranking compounds in order of acidity; acid/base reactions with carboxylic acids; extraction (laboratory separation technique). Carbonation (reaction of Grignard reagent with carbon dioxide to form carboxylic acid). Reduction of carboxylic acids with lithium aluminum hydride (LiAlH4) to form alcohols. Reaction of carboxylic acids with SOCl2 (thionyl chloride) to form acyl chlorides. Decarboxylation This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: www.freelance- For a printable document containing the handout discussed in this video series, go to my website. For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: (1) Acidity of carboxylic acids (2) Continued. Ranking compounds in order of acidity (3) Continued (4) Continued. Acid/base reactions of carboxylic acids (5) Continued (6) Extraction (laboratory separation technique) (7) Carbonation (attack of Grignard reagent on carbon dioxide to form carboxylic acid) (8) Reduction of aldehydes and ketones with lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) to form alcohols (9) Reduction of carboxylic acids with lithium aluminum hydride to form alcohols (10) Continued (11) Reaction of ...
  • Aclara automatic meter reading (AMR) units rely on Tadiran Batteries Twenty-five years ago, Aclara™ (formerly Hexagram,Inc.) installed hundreds of thousands automatic meter reading (AMR) devices for the utility market. Powered by a Tadiran TL-2100 AA-size lithium thionyl chloride battery, virtually all of these decades-old devices are still operating on their original battery, validated by laboratory tests confirming that these cells have retained nearly 25% of their original capacity. Glenn Emelko, Director of Technology, discusses why Aclara continues to choose Tadiran TL-4903 lithium batteries for use in their STAR® Network wireless fixed-network AMR units. Aclara selected Tadiran batteries based on superior performance characteristics, including higher energy density, higher capacity, a temperature range of 55ºC to +85ºC., and 20+ year service life.
  • Activated Alcohols: A Good Leaving Group from a Poor One This webcast describes transformations of the alcohol hydroxyl group from a poor leaving group to a good leaving group.
  • Carboxylic Acid to Amide Derivative: Part 1 After brewing thionyl chloride with my unknown liquid (which I believed to be a carboxylic acid), I used a Pasteur pipet to dispense this mixture dropwise into ice-cold concentrated ammonium hydroxide. It was a very showy, exothermic reaction and sparks could be seen inside the beaker early on. I didn't think to record video until halfway through the reaction. The reaction is on pages 971-972 in our lab textbook.
  • Lec 11 | MIT 5.111 Principles of Chemical Science, Fall 2008 Lecture 11: Lewis structures License: Creative Commons BY-NC-SA More information at ocw.mit.edu More courses at ocw.mit.edu
  • Make a Lithium Thionyl Chloride Battery How to make a Lithium Thionyl Chloride Battery capable of generating 2.8v with enough current to power a LED. Warning: Thionyl Chloride is EXTREMELY toxic and this experiment must be performed in a fumehood by an experienced chemist with proper safety precautions. Lithium thionyl chloride batteries offer excellent shelf life (sometimes over a decade) and energy density. Their main drawback is they are not rechargeable but for low power applications like memory backup they are extremely useful. At very low power levels, they can outlast the device they are installed in, making the recharge issue a non-issue. As seen in this experiment, they are also extremely simple to make. A solution of lithium tetrachloroaluminate in thionyl chloride serves as the electrolyte and the lithium and carbon rods are simply inserted in. The cell can produce up to 3.5volts depending on the purity and quality of the components. Our cell in the video used waste chemicals we had leftover around the lab so the voltage is not that high. But it did produce enough power to light a small light emitting a diode. Commercial cells use lithium foil and spongy carbon for greater current but the concept is still the same. Our website at:
  • BeanAir - Wireless Temperature and Humidity Sensor • Temperature sensor (PT1000) & Humidity (capacitive technology) • Temperature measurement range : -25°C to +85°C • Humidity measurement range : 0...100 %RH • Ultra-low power consumption technology Zigbee®/IEEE 802.15.4 : Current consumption in idle mode less than 13 uA • Option : Barometric pressure measurement 10 mBar....1100 mBar • Radio range : 70 m to 1 km (LOS) • Embedded Logger : up to 1000 000 measurement records • Entirely autonomous system : function on Lithium-thionyl chloride primary battery, on Lithium-Ion rechargeable battery, or on external power source • « Plug and Play » installation : the temperature/ humidity sensor does not need any calibration • Calibration free on the temperature/humidity probe Applications: Cold chain traceability, Air-conditionning System (HVAC), Medical lab & white room, Technical Building Management, Process Monitoring, Transport
  • FURSCA Day 3 Adding Thionyl Chloride (SOCl2) as a step in making an iodophenyl oxazoline. If you look closely, you can see the SOCl2 fume as I open the bottle and inside the flask. Thionyl Chloride reacts violently with water, including the vapor in the air, producing HCl gas.
  • Lec 12 | MIT 5.111 Principles of Chemical Science, Fall 2005 Lewis Diagrams (Prof. Sylvia Ceyer) View the complete course: ocw.mit.edu License: Creative Commons BY-NC-SA More information at ocw.mit.edu More courses at ocw.mit.edu

Blogs & Forum
blogs and forums about thionyl

  • “Welcome to the Chemistry forum. Join the conversation. Here we know Thionyl chloride is a component of prototype lithium-thionyl chloride batteries, where it forms the anode with lithium as the cathode”
    — Lithium Thionyl Chloride batteries - Chemistry,

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  • “battbase.over- hébergé par OverBlog With lithium as the anode, cathode and electrolyte is thionyl chloride (thionyl chloride), cylinder-type battery,Acer Aspire 1410 Battery, the assembly was finished, a power, voltage 3.6V, is the most stable operating voltage of the battery types”
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  • “Source: Tadiran Batteries are the lifeblood of a wireless device, providing the essential power Lithium thionyl chloride batteries have a proven track record for utility metering applications”
    — element14: TechFirst: Batteries for Smart Gas Meters, element-14.com

  • “The following information is about passivation of lithium thionyl chloride battery for the That is to say, the active matter lithium and thionyl chloride that are used for”
    — DATE:,

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  • “Latest ideas about Lithium Batteries - Commonly Used In Most Portable Electronic Devices. Hear it from first. Lithium-thionyl chloride batteries find use in commercial/industrial applications, or are installed into devices where no consumer replacement is performed”
    — Lithium Batteries - Commonly Used In Most Portable Electronic,

  • “Lithium Batteries Toronto, Ontario, Canada, USA One type of lithium cell having a large energy density is the lithium-thionyl chloride cell. In this cell, a liquid mixture of thionyl chloride and lithium tetrachloroaluminate acts as the cathode and electrolyte respectively”
    — Lithium Batteries Toronto, Ontario, Canada, USA, 911gear.ca

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